4-(1,3-Dioxoisoindolin-2-yl)butanal

95%

Reagent Code: #177183
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CAS Number 3598-60-5

science Other reagents with same CAS 3598-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.22 g/mol
Formula C₁₂H₁₁NO₃
badge Registry Numbers
MDL Number MFCD00454178
thermostat Physical Properties
Boiling Point 373.9 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.274 g/cm3(Predicted)
Storage -20°C, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of phthalimide derivatives with biological activity. It serves as a building block in pharmaceuticals and agrochemicals due to its reactive aldehyde group and cyclic imide structure. The compound is also employed in the development of fluorescent probes and dyes, where its conjugated system enhances optical properties. Its bifunctional nature allows for use in cross-coupling reactions and the formation of heterocyclic compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,650.00
inventory 250mg
10-20 days ฿29,300.00
inventory 1g
10-20 days ฿98,890.00

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4-(1,3-Dioxoisoindolin-2-yl)butanal
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Used as an intermediate in organic synthesis, particularly in the preparation of phthalimide derivatives with biological activity. It serves as a building block in pharmaceuticals and agrochemicals due to its reactive aldehyde group and cyclic imide structure. The compound is also employed in the development of fluorescent probes and dyes, where its conjugated system enhances optical properties. Its bifunctional nature allows for use in cross-coupling reactions and the formation of heterocyclic compounds

Used as an intermediate in organic synthesis, particularly in the preparation of phthalimide derivatives with biological activity. It serves as a building block in pharmaceuticals and agrochemicals due to its reactive aldehyde group and cyclic imide structure. The compound is also employed in the development of fluorescent probes and dyes, where its conjugated system enhances optical properties. Its bifunctional nature allows for use in cross-coupling reactions and the formation of heterocyclic compounds.

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